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Victorian Intergenerational Health Cohort Study (VIHCS)
Victorian Intergenerational Health Cohort Study logo
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Sample details

VIHCS is the second of the two 2000 Stories Study cohorts based in Victoria, Australia. VIHCS follows 1,030 children of the Victorian Adolescent Health Cohort Study (VAHCS) participants. The parents have been contacted at four times: during pregnancy, two months after birth, at their child’s first birthday, and as their child turned eight years old, and the children will be contacted at age 15 years for the fifth wave of VIHCS. This will be an exciting opportunity to check in with the VIHCS kids at the same age as their parents were when they began taking part in the study.

Study design
Cohort, Cohort - birth, Cohort - intergenerational

Number of participants at first data collection

665 (parents)

1,030 (children)

Age at first data collection

12 - 18 weeks gestation (parents)

Birth (children)

Participant year of birth

Varied (parents)

2006 - 2013 (children)

Participant sex
All

Representative sample at baseline?
No

Sample features

Adolescents
Caregiver and child dyad
Children and young people
Families
Intergenerational
Dataset details

Country

Australia

Year of first data collection

2006

Primary Institutions

King's College London (KCL)

University College London (UCL)

Links

mcri.edu.au/research/projects/2000-stories

lifecourse.melbournechildrens.com/cohorts/2000-stories/

rch.org.au/cah/research/2000_Stories/

Profile paper DOI

doi.org/10.1111/ppe.12602

Funders

National Health and Medical Research Council (NHMRC)

Australian Federal Government Department of Health and Ageing

Australian Rotary Health (ARH)

Murdoch Children's Research Institute (MCRI)

VicHealth

Ongoing?
Yes

Data types collected

mentalHealthData
dataLinkage
Quantitative data collection
  • Computer, paper or task testing (e.g. cognitive testing, theory of mind doll task, attention computer tasks)
  • Interview – phone
  • Physical or biological assessment (e.g. blood, saliva, gait, grip strength, anthropometry)
  • Self-report questionnaire – online
  • Self-report questionnaire – paper or computer assisted
Qualitative data collection
  • None
Neuroimaging data collection
  • None
Linked or secondary data
  • Education data
  • Healthcare data
  • Medical birth registry
Features

Engagement

  • None
  • Keywords

    Biological samples/biospecimens
    Childhood
    Environment
    Family environment and factors
    Human development
    Infancy and early childhood
    Intergenerational
    Lifecourse
    Neurocognitive development
    Parental mental health
    Physical activity and exercise
    Physical health
    Socioeconomics

    Consortia and dataset groups

    2000 Stories Study
    Australian and New Zealand Intergenerational Cohort Consortium (ANZ-ICC)
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